传出细胞增多
免疫抑制
败血症
炎症
免疫学
医学
巨噬细胞
重症监护医学
生物
生物化学
体外
作者
Xiaoyu Guo,Peiming Shen,Rongjiao Shao,Ting Hong,Weizhuo Liu,Yi Shen,Fan Su,Qinlan Wang,Bin He
标识
DOI:10.1088/1748-605x/acef9a
摘要
Abstract Uncontrolled inflammation storm induced by sepsis may lead to severe organ dysfunction and secondary immunosuppression, which is one of the main reasons for high mortality and prolonged hospitalization of septic patients. However, there is a lack of effective treatments for it at present. Here, we report an efferocytosis-inspired nanodrug (BCN@M) to treat sepsis and secondary immunosuppression via regulating the macrophage function. Bioactive molecular curcumin was loaded with bovine serum albumin and then coated with the damaged erythrocyte membrane derived from septic mice. It was found that the septic erythrocytes promoted the efferocytosis signal and BCN@M uptake efficiency by macrophages. The well-constructed BCN@M nanodrug reduced the hyperinflammation in sepsis and restored the bacterial clearance ability of macrophage in the secondary immunosuppression state. This study highlights BCN@M as an efferocytosis-inspired nanodrug to alleviate hyperinflammation and secondary immunosuppression of sepsis.
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